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143982-54-1

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143982-54-1 Usage

General Description

Ethyl 3-bromoimidazo[1,2-a]pyridine-2-carboxylate is a chemical compound with the molecular formula C9H7BrN2O2. It is a derivative of imidazo[1,2-a]pyridine, a heterocyclic compound with potential biological activities. This specific compound is often used in organic synthesis and medicinal chemistry as a building block for creating other pharmaceutical or biologically active molecules. It is important to handle and store this compound carefully, as it may pose certain health and safety risks if not used properly. Overall, Ethyl 3-bromoimidazo[1,2-a]pyridine-2-carboxylate is a versatile compound with potential applications in various fields of research and industry.

Check Digit Verification of cas no

The CAS Registry Mumber 143982-54-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,9,8 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 143982-54:
(8*1)+(7*4)+(6*3)+(5*9)+(4*8)+(3*2)+(2*5)+(1*4)=151
151 % 10 = 1
So 143982-54-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H7BrN2O2/c1-14-9(13)7-8(10)12-5-3-2-4-6(12)11-7/h2-5H,1H3

143982-54-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 3-Bromoimidazo[1,2-a]pyridine-2-carboxylate

1.2 Other means of identification

Product number -
Other names Ethyl 3-bromoimidazo[1,2-a]pyridine-2-carboxylate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:143982-54-1 SDS

143982-54-1Relevant articles and documents

Chemodivergent synthesis of: N -(pyridin-2-yl)amides and 3-bromoimidazo[1,2- a] pyridines from α-bromoketones and 2-aminopyridines

Liu, Yanpeng,Lu, Lixue,Zhou, Haipin,Xu, Feijie,Ma, Cong,Huang, Zhangjian,Xu, Jinyi,Xu, Shengtao

, p. 34671 - 34676 (2019/11/13)

N-(Pyridin-2-yl)amides and 3-bromoimidazo[1,2-a]pyridines were synthesized respectively from α-bromoketones and 2-aminopyridine under different reaction conditions. N-(Pyridin-2-yl)amides were formed in toluene via C-C bond cleavage promoted by I2/s

Identification of fused bicyclic heterocycles as potent and selective 5-HT2A receptor antagonists for the treatment of insomnia

Xiong, Yifeng,Ullman, Brett,Choi, Jin-Sun Karoline,Cherrier, Martin,Strah-Pleynet, Sonja,Decaire, Marc,Feichtinger, Konrad,Frazer, John M.,Yoon, Woo H.,Whelan, Kevin,Sanabria, Erin K.,Grottick, Andrew J.,Al-Shamma, Hussien,Semple, Graeme

, p. 1870 - 1873 (2012/04/17)

A series of fused bicyclic heterocycles was identified as potent and selective 5-HT2A receptor antagonists. Optimization of the series resulted in compounds that had improved PK properties, favorable CNS partitioning, good pharmacokinetic properties, and significant improvements on deep sleep (delta power) and sleep consolidation.

Pyrrolization processes of vinyl substituted imidazo[1,2-a]pyridine, pyrimidine and 1,8-naphthyridine

Chavignon,Teulade,Madesclaire,Gueiffier,Blache,Viols,Chapat,Dauphin

, p. 691 - 697 (2007/10/02)

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